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4-phenyl-2-(4-phenyl-1,3-thiazol-2-yl)-1,3-thiazole is a complex organic compound characterized by its unique molecular structure. It is a heterocyclic compound, specifically a derivative of thiazole, which is a five-membered ring containing sulfur and nitrogen atoms. This particular compound features two thiazole rings, one of which is substituted with a phenyl group at the 4-position, while the other is connected to the first ring at the 2-position. The presence of phenyl groups imparts stability and aromaticity to the molecule, which can influence its chemical properties and potential applications. 4-phenyl-2-(4-phenyl-1,3-thiazol-2-yl)-1,3-thiazole may be of interest in the fields of organic chemistry and materials science, particularly in the development of new pharmaceuticals, dyes, or other specialty chemicals due to its structural complexity and potential for diverse interactions.

4072-63-3

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4072-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4072-63-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4072-63:
(6*4)+(5*0)+(4*7)+(3*2)+(2*6)+(1*3)=73
73 % 10 = 3
So 4072-63-3 is a valid CAS Registry Number.

4072-63-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-phenyl-2-(4-phenyl-1,3-thiazol-2-yl)-1,3-thiazole

1.2 Other means of identification

Product number -
Other names 4,4'-diphenyl-2,2'-bithiazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4072-63-3 SDS

4072-63-3Downstream Products

4072-63-3Relevant academic research and scientific papers

Synthesis and structure of boron-bithiazole complexes

Findlater, Michael,Swisher, Nicholas S.,White, Peter S.

, p. 5379 - 5382 (2010)

The syntheses of the first reported p-block complexes of the bithiazole moiety are reported, namely [(tBuBTz)BBr2][Br] (3), and [(PhBTz)BBr2][Br] (4) (tBuBTz = 4,4′-di-tert-butyl-2,2′- bithiazole and PhBTz = 4,4′-diphenyl-2,2′-bithia

Palladium-Catalyzed Reactions of Terminal Acetylenes and Olefins with Halo-1,3-azoles

Sakamoto, Takao,Nagata, Hideo,Kondo, Yoshinori,Shiraiwa, Masafumi,Yamanaka, Hiroshi

, p. 823 - 828 (2007/10/02)

The palladium-catalyzed reactions of 4-bromo- and 5-bromothiazoles, as well as 4-bromo and 5-bromooxazoles with terminal acetylenes gave ethynyl derivatives in 43-89percent yields, whereas the reactions of 2-bromothiazoles and iodo-N-methylimidazoles affo

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